[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Cumhuriyet University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":574},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,21,0,[8,49,79,102,129,154,183,210,237,262,291,321,346,370,397,426,456,481,507,534,551],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100644620","comparson-of-analgesc-effcacy-of-dfferent-volumes-of-serratus-posterior-superor-intercostal-plane-block-after-modfed-radcal-mastectomy-surgery-100644620",false,"NCT07670078","Comparıson of Analgesıc Effıcacy of Dıfferent Volumes of Serratus Posterior Superıor Intercostal Plane Block After Modıfıed Radıcal Mastectomy Surgery","Comparıson of Analgesıc Effectıveness of Dıfferent Volumes of Serratus Posterıor Superıor Intercostal Plane Block In Patıents Undergoıng Modıfıed Radıcal Mastectomy Surgery","Inclusion Criteria:\n\n* The study included adult patients over 18 years of age who underwent modified radical mastectomy under general anesthesia and were classified in risk groups I-II-III according to the American Society of Anesthesiologists (ASA) risk classification.\n\nExclusion Criteria:\n\n* patients with coagulopathy,\n* patients with signs of infection at the block application site,\n* patients with ASA IV\n* patients with known allergies to any of the study drugs,\n* patients with ineffective block\n* patients who could not cooperate during postoperative pain assessment\n* patients who wanted to withdraw from the study,\n* patients with alcohol and drug addiction,\n* patients with musculoskeletal abnormalities\n* patients with kidney and liver failure\n* patients with obesity (body mass ≥ 35 kg\u002Fm2)","FEMALE","18 Years","65 Years",{"count":20,"type":21},90,"ESTIMATED","INTERVENTIONAL",[24],"NA","The aim of researchers is to compare the effects of three different local anesthetic concentrations and volumes on opioid consumption, postoperative analgesic efficacy, and pain scores during ultrasound-guided SPSIP blocks in patients undergoing modified radical mastectomy. Additionally, we aim to map and identify the dermatomal areas where different concentrations and volumes of SPSIP blocks provide analgesia.",[27,28,29],"Modified Radical Mastectomy","Post Operative Pain, Acute","Facial Plane Blocks",[31,32,33,34,35],"postoperative pain","regional anesthesia","Modified radical mastectomy","opioid free analgesia","facial plan block","NOT_YET_RECRUITING","2026-06-25",{"date":39,"type":40},"2026-06-29","ACTUAL",{"date":42,"type":21},"2026-08-15",{"date":44,"type":21},"2027-08-30",{"name":46,"class":47},"Cumhuriyet University","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":4,"enrollmentInfo":59,"targetDuration":61,"studyType":62,"phases":4,"briefSummary":63,"conditions":64,"keywords":66,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":48},"100644220","evaluation-of-adverse-effects-related-to-prescribed-medications-in-a-periodontology-clinic-100644220","NCT07666100","Evaluation of Adverse Effects Related to Prescribed Medications in a Periodontology Clinic","Evaluation of Adverse Effects Related to Prescribed Medications in a Periodontology Clinic in Terms of Causality, Severity, and Quality of Life: A Prospective Study","Inclusion Criteria:\n\nBeing 16 years of age or older\n\n* Receiving treatment at a periodontology clinic • Having been prescribed at least one pharmacological agent\n* Volunteering to participate in the study and providing informed consent\n\nExclusion Criteria:\n\n* Having a cognitive problem that would prevent the evaluation of side effects related to drug use\n\n  * Patients who did not come for evaluation during the follow-up period or for whom sufficient follow-up data could not be obtained\n  * Patients who provided incomplete, inconsistent or unreliable data regarding side effect evaluation",true,"ALL","16 Years",{"count":60,"type":21},571,"10 Days","OBSERVATIONAL","Various pharmacological treatment approaches, primarily antibiotics, analgesics, and antiseptic agents, are frequently used in the treatment of periodontal diseases. While these drugs are important for the clinical effectiveness of periodontal treatment, drug-related side effects can negatively impact patient compliance, quality of life, and overall patient safety, and in some cases, may lead to premature termination of treatment. Early identification of drug-related side effects, assessment of causality, and classification of severity form the basis of pharmacovigilance practices. In this context, the Adverse Event Reporting System (FAERS), run by the United States Food and Drug Administration (FDA), is an important data source for detecting drug-related side effects and presenting safety signals. Large databases like FAERS draw attention to potential drug-related side effects and provide valuable information on drug safety. However, this data is largely based on patient\u002Fuser or physician feedback, and these systems are insufficient to assess the true frequency, clinical severity, and impact on patients' quality of life of side effects.\n\nSide effects related to medications prescribed in periodontology clinics are often considered mild or transient, thus limiting systematic feedback based on real-life data. Therefore, systematic and patient-centered clinical studies using standard algorithms and scales based on real-life data are needed. This study aims to determine the frequency of side effects related to medications prescribed in a periodontology clinic over an 18-month period and to evaluate them according to gender and age. As a secondary aim, it aims to evaluate the causal relationship of these side effects with the medications, their clinical severity, and their impact on patients' quality of life related to oral health using a holistic approach.\n\nThis will ensure that not only the presence of side effects but also clinical and patient-centered outcomes are presented in an objective, standardized, and reproducible manner.",[65],"Having a Periodontal Prescription",[67,68,69],"adverseeffect","pharmocovigiliance","Periodontology","RECRUITING","2026-06-23",{"date":73,"type":40},"2026-06-26",{"date":75,"type":40},"2026-03-30",{"date":77,"type":21},"2027-09-30",{"name":46,"class":47},{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":56,"sex":57,"minAge":17,"maxAge":18,"enrollmentInfo":86,"targetDuration":4,"studyType":62,"phases":4,"briefSummary":88,"conditions":89,"keywords":92,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":48},"100641321","surgical-positions-and-postoperative-atelectasis-a-lung-ultrasound-study-100641321","NCT07654153","Surgical Positions and Postoperative Atelectasis: A Lung Ultrasound Study","Evaluation of the Effect of Surgical Positions Under General Anesthesia on Postoperative Atelectasis Using Lung Ultrasonography","Inclusion Criteria:\n\n* Being between 18-65 years of age\n* Having ASA I-III status\n* Planning elective surgery under general anesthesia\n* Agreeing to participate in the study and signing the consent form\n\nExclusion Criteria:\n\n* Patients requiring emergency surgery\n* Patients with ASA IV or higher\n* Presence of a known serious preoperative lung disease (COPD, Asthma, Pneumonia, Pleural effusion, Pneumothorax, Interstitial lung disease, Bronchiectasis, etc.)\n* History of neuromuscular disease\n* Body Mass Index (BMI) \\> 35 kg\u002Fm² (Morbid obesity)\n* Presence of chest wall deformity or skin lesions that would obstruct LUS imaging\n* Cases with an operative duration of less than 60 minutes or more than 300 minutes\n* Patients with a history of thoracotomy, sternotomy, or prior open thoracic surgery\n* Patients with alcohol or drug dependence\n* Patients with significant anemia\n* Patients who are pregnant or lactating\n* Patients who develop laryngospasm following extubation\n* Refusal to provide consent or inability to cooperate",{"count":87,"type":21},100,"The aim of this study is to prospectively evaluate the effect of surgical position on the development of postoperative atelectasis in patients undergoing surgery in supine, prone, lateral decubitus, and lithotomy positions using lung ultrasonography (LUS), and to investigate whether there is a difference between these positions.",[90,91],"Lung Ultrasound","Atelectasis",[93],"lung ultrasound","2026-06-18",{"date":96,"type":40},"2026-06-22",{"date":98,"type":21},"2026-07-20",{"date":100,"type":21},"2027-08-01",{"name":46,"class":47},{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":57,"minAge":17,"maxAge":4,"enrollmentInfo":109,"targetDuration":4,"studyType":22,"phases":111,"briefSummary":112,"conditions":113,"keywords":115,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":128},"100633283","comprasion-of-spsip-and-rhomboid-intercostal-plan-blocks-on-vats-100633283","NCT07524673","Comprasion of SPSIP and Rhomboid Intercostal Plan Blocks on VATS","Comparison of the Analgesic Efficacy of Rhomboid Intercostal Plane Block and Serratus Posterior Superior Intercostal Plane Block on Postoperative Pain in Patients Undergoing Video-Assisted Thoracoscopic Surgery","Inclusion Criteria:\n\n* Forty adult patients scheduled for elective wedge resection or biopsy under VATS, classified as American Society of Anesthesiologists (ASA) physical status I-III, were enrolled after providing written informed consent.\n\nExclusion Criteria:\n\n* ASA class IV or higher,\n* morbid obesity (BMI \\> 40 kg\u002Fm²),\n* body weight ≤ 50 kg,\n* skin infection at the block site,\n* refusal to participate,\n* inability to cooperate during postoperative pain assessment,\n* conversion to open surgery,\n* preexisting pain,\n* known allergy to any study medication,\n* coagulopathy.",{"count":110,"type":21},40,[24],"This study aimed to compare rhomboid intercostal plane block and serratus posterior superior intercostal plane block (SPSIPB) to determine the most suitable technique for maintaining postoperative analgesia in video-assisted thoracoscopic surgeries (VATS).",[114],"Postoperative Pain Management",[116,117,118,119,31],"rhomboid intercostal plane block","serratus posterior superior intercostal plane block","vats","video-assisted thoracoscopic surgery","2026-06-02",{"date":122,"type":40},"2026-06-03",{"date":124,"type":40},"2026-03-12",{"date":126,"type":21},"2026-12",{"name":46,"class":47},2,{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":4,"eligibilityCriteria":135,"healthyVolunteers":11,"sex":57,"minAge":17,"maxAge":18,"enrollmentInfo":136,"targetDuration":4,"studyType":22,"phases":138,"briefSummary":139,"conditions":140,"keywords":143,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":148,"startDateStruct":149,"completionDateStruct":151,"leadSponsor":153,"locationsCount":48},"100608615","the-effectiveness-of-quadro-liac-plane-block-in-percutaneous-nephrolithotomies-100608615","NCT07203859","The Effectiveness of Quadro İliac Plane Block in Percutaneous Nephrolithotomies","Comparison of the Effects of Ultrasound-Guided Quadro-İliac Plane Block on Postoperative Pain Level and Analgesia Requirement in Patients Undergoing Percutaneous Nephrolithotomy","Inclusion Criteria:\n\n* Adult patients over 18 years of age who underwent percutaneous nephrolithotomy under general anesthesia and were I-II-III according to the American Society of Anesthesiologists (ASA) risk classification were included in the study.\n\nExclusion Criteria:\n\n* patients who did not give consent,\n* patients with coagulopathy,\n* patients with signs of infection at the block application site,\n* patients using anticoagulants,\n* patients with known allergies to any of the study drugs,\n* patients with unstable hemodynamics,\n* patients who could not cooperate during postoperative pain assessment\n* patients who wanted to withdraw from the study,\n* patients with alcohol and drug addiction,\n* patients with musculoskeletal abnormalities",{"count":137,"type":21},60,[24],"Our aim was to investigate the effect of quadro iliac plane block on postoperative analgesia in patients undergoing percutaneous nephrolithotomy surgery and to determine which areas of the skin this block anesthetizes.",[141,142],"Postoperative Pain","Percutaneous Nephrolithotomy",[31,32,144,145,34,146,147],"percutaneous nephrolithotomy","quadroiliac plane block","ibuprofen","novel fascial plane block",{"date":122,"type":40},{"date":150,"type":40},"2025-09-25",{"date":152,"type":21},"2026-10",{"name":46,"class":47},{"id":155,"slug":156,"hasResults":11,"nctId":157,"briefTitle":158,"officialTitle":159,"acronym":4,"eligibilityCriteria":160,"healthyVolunteers":56,"sex":57,"minAge":17,"maxAge":161,"enrollmentInfo":162,"targetDuration":4,"studyType":22,"phases":164,"briefSummary":165,"conditions":166,"keywords":170,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":176,"lastUpdatePostDateStruct":177,"startDateStruct":179,"completionDateStruct":181,"leadSponsor":182,"locationsCount":48},"100634079","the-effect-of-mandala-art-therapy-psychological-resilience-coping-with-cancer-colorectal-cancer-surgery-100634079","NCT07535021","The Effect of Mandala Art Therapy, Psychological Resilience, Coping With Cancer, Colorectal Cancer Surgery","The Effect of Mandala Art Therapy on Psychological Resilience and Coping With Cancer in Patients Undergoing Colorectal Cancer Surgery: a Prospective Randomized Controlled Study.","Inclusion Criteria:\n\n* To communicate,\n* Aged 18 or older,\n* Agreed to participate\n* Scheduled for colorectal cancer surgery.\n* No physical disability of the upper extremities,\n* no visual problems,\n* no history of psychotic drug use,\n* pain intensity and fatigue level ≤3 points according to VAS-10 before MST application,\n* will be hospitalized for 3 days postoperatively,\n\nExclusion Criteria:\n\n* Over 74 years old,\n* has not completed mandala art therapy application,\n* is not compliant with the application,\n* has a history of previous psychiatric diagnosis.","74 Years",{"count":163,"type":21},70,[24],"The aim of this study is to evaluate the effects of mandala art therapy on psychological resilience and coping with cancer in patients undergoing colorectal cancer surgery.\n\nThis study was conducted as a randomized controlled trial with a pre-test-post-test design, including intervention and control groups. The study will be conducted between January 2026 and December 2026 with patients undergoing colorectal cancer surgery. The G.power 3.1.9.7 program was used for sample size calculation. The sample size was determined as 28 individuals in each group, considering equal sample sizes in the experimental and control groups, a 95% confidence interval (type I error 5%), and statistical power of 80% (type II error 20%) with an effect size of d=0.50. However, considering a possible 20% data loss, 35 individuals will be included in each group, resulting in a total sample size of 70 individuals.\n\nSample selection will be made using sequential sampling according to inclusion criteria. Patients will then be randomly assigned to the experimental group (A) and the control group (B) using block randomization (four-block). First, 15 blocks of four, such as AABB, ABAB, ABBA, BBAA, BABA, BAAB, etc., will be prepared by the researcher and statistician. Individuals will then be divided into two groups according to the prepared list; this process will be repeated continuously until the sample size is complete.\n\nThree data collection forms were used. SPSS 22.00 software package was used for data analysis. Skewness and kurtosis analyses were performed to determine the normality of the data distribution. Frequency (n) and percentage (%) distributions were calculated to determine the sociodemographic and clinical characteristics of the participants. Independent samples t-test was used to determine the mean differences between two independent groups, dependent samples t-test was used to compare pre- and post-intervention measurements, and repeated measures one-way analysis of variance (ANOVA) was used. Cohen's d effect size was calculated to evaluate the significance of the difference between groups in terms of the intervention. The statistical significance level was accepted as p\\\u003C0.05.",[167,168,169],"Colorectal Cancer","Coping, Cognitive","Psychological Well-Being",[171,172,173,174,175],"colorectal cancer","cope with cancer","psychological resilience","mandala art therapy","nursing care","2026-04-10",{"date":178,"type":40},"2026-04-16",{"date":180,"type":40},"2026-01-01",{"date":126,"type":21},{"name":46,"class":47},{"id":184,"slug":185,"hasResults":11,"nctId":186,"briefTitle":187,"officialTitle":187,"acronym":4,"eligibilityCriteria":188,"healthyVolunteers":56,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":189,"targetDuration":4,"studyType":22,"phases":190,"briefSummary":191,"conditions":192,"keywords":197,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":202,"lastUpdatePostDateStruct":203,"startDateStruct":205,"completionDateStruct":207,"leadSponsor":209,"locationsCount":48},"100629417","the-effect-of-a-multi-component-breastfeeding-support-program-on-breastfeeding-self-efficacy-and-mother-infant-bonding-in-mothers-following-cesarean-section-100629417","NCT07474402","The Effect of a Multi-Component Breastfeeding Support Program on Breastfeeding Self-Efficacy and Mother-Infant Bonding in Mothers Following Cesarean Section","Inclusion Criteria:\n\n\\- Primiparous mothers who have completed pregnancy\n\nMothers who delivered by cesarean section (C\u002FS)\n\nMothers in the early postpartum period\n\nMothers aged 18 years and older\n\nMothers who are exclusively breastfeeding\n\nMothers with healthy and stable infants\n\nMothers with no medical conditions that may interfere with breastfeeding\n\nMothers who can read and understand Turkish and complete the data forms\n\nExclusion Criteria:\n\n* Mothers who experienced postpartum complications\n\nInfants with severe health problems, congenital anomalies, or requiring intensive care\n\nInfants hospitalized in neonatal intensive care unit\n\nMothers with medical or psychiatric conditions that prevent breastfeeding\n\nMothers with multiple pregnancies (twins, triplets, etc.)\n\nMothers who cannot attend follow-up visits during the study\n\nMothers without mobile phones\n\nMothers who received breastfeeding education during pregnancy",{"count":87,"type":21},[24],"This study tests a breastfeeding support program for mothers who give birth by cesarean section. The purpose of the study is to see whether the program helps mothers feel more confident about breastfeeding and improves mother-baby bonding.",[193,194,195,196],"Breastfeeding Self-Efficacy","Mother-Infant Attachment","Breastfeeding Consultancy Training","Primigravida Women",[198,193,199,200,201],"Cesarean Section","Maternal-Infant Bonding","Breastfeeding Support","Postpartum Period","2026-03-21",{"date":204,"type":40},"2026-03-25",{"date":206,"type":40},"2026-02-20",{"date":208,"type":21},"2026-11-30",{"name":46,"class":47},{"id":211,"slug":212,"hasResults":11,"nctId":213,"briefTitle":214,"officialTitle":214,"acronym":4,"eligibilityCriteria":215,"healthyVolunteers":56,"sex":57,"minAge":4,"maxAge":4,"enrollmentInfo":216,"targetDuration":4,"studyType":22,"phases":218,"briefSummary":219,"conditions":220,"keywords":223,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":229,"lastUpdatePostDateStruct":230,"startDateStruct":232,"completionDateStruct":234,"leadSponsor":236,"locationsCount":48},"100615905","the-effect-of-benners-jigsaw-teaching-technique-based-on-the-novice-to-expert-model-and-scenario-based-peripheral-intravenous-catheterization-instruction-on-skill-acquisition-of-nursing-students-an-experimental-study-100615905","NCT07298681","The Effect of Benner's Jigsaw Teaching Technique Based on the Novice to Expert Model and Scenario-Based Peripheral Intravenous Catheterization Instruction on Skill Acquisition of Nursing Students: An Experimental Study.","Inclusion Criteria:\n\n* Volunteering to participate in research\n* To be a first-year Nursing student\n* To be taking the Nursing Fundamentals-II course for the first time\n* To be a smart phone or computerVolunteering to participate in resrs a day\n\nExclusion Criteria:\n\n* Being a foreign national (due to the risk of having language problems)\n* To have received high school and associate degree education in the field of Public health",{"count":217,"type":21},80,[24],"This randomized controlled experimental study aims to evaluate the effectiveness of a training program based on the Jigsaw teaching technique and scenario-based learning in improving the peripheral intravenous catheterization skill levels of first-year nursing students. Participants will be randomly assigned to either the intervention group, receiving Jigsaw-based collaborative learning combined with clinical scenarios, or the control group receiving traditional skills training. The primary outcome is the improvement in students' clinical skill performance as measured by a standardized skill assessment checklist. The study seeks to determine whether innovative, active learning methods can enhance fundamental nursing skills training",[221,222],"Nursing Education","Clinical Skills Training",[224,225,226,227,228],"jigsaw","scenario-based training","skills training","nurse","intravenous catheter","2026-03-17",{"date":231,"type":40},"2026-03-19",{"date":233,"type":40},"2026-02-24",{"date":235,"type":21},"2027-06-30",{"name":46,"class":47},{"id":238,"slug":239,"hasResults":11,"nctId":240,"briefTitle":241,"officialTitle":242,"acronym":4,"eligibilityCriteria":243,"healthyVolunteers":11,"sex":16,"minAge":244,"maxAge":18,"enrollmentInfo":245,"targetDuration":4,"studyType":22,"phases":246,"briefSummary":247,"conditions":248,"keywords":250,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":255,"lastUpdatePostDateStruct":256,"startDateStruct":257,"completionDateStruct":259,"leadSponsor":261,"locationsCount":48},"100630027","effects-of-core-stabilization-exercises-in-female-patients-with-gonarthrosis-100630027","NCT07482332","Effects of Core Stabilization Exercises in Female Patients With Gonarthrosis","Randomized Controlled Study of the Effects of Core Stabilization Exercises in Addition to Knee Exercises in Female Patients With Gonarthrosis","Inclusion Criteria:\n\n* Kellgren-Lawrence 2-3 knee osteoarthritis\n* Female patient aged 40-65\n* Volunteer\n\nExclusion Criteria:\n\n* Having received physical therapy within the last month\n* Presence of neurological, cardiac, and respiratory problems\n* Less than 90 degrees of flexion in the knee and hip joints\n* Presence of any pathology in the lower extremity that may affect balance and function\n* History of lower extremity surgery\n* Severe visual, hearing, and speech impairment\n* Illiteracy in Turkish\n* Body mass index of 30 or higher","45 Years",{"count":110,"type":21},[24],"Osteoarthritis (OA) is a non-inflammatory degenerative disease characterized by progressive deterioration of cartilage tissue, synovial membrane, and joint capsule, primarily affecting weight-bearing joints. Individuals with knee osteoarthritis exhibit weakness in the trunk and periarticular muscles. This loss of strength in the trunk and periarticular muscles increases the load on the joint, contributing to the development and progression of the disease. This study aimed to investigate the effects of core stabilization, applied in addition to knee muscle exercise programs, on clinical symptoms and functional capacity in individuals with knee osteoarthritis.",[249],"Knee Osteoarthritis (Knee OA)",[251,252,253,254],"Knee osteoarthritis","Core stabilization exercise","Physiotherapy","Function","2026-03-16",{"date":231,"type":40},{"date":258,"type":40},"2026-01-05",{"date":260,"type":21},"2026-09-14",{"name":46,"class":47},{"id":263,"slug":264,"hasResults":11,"nctId":265,"briefTitle":266,"officialTitle":267,"acronym":4,"eligibilityCriteria":268,"healthyVolunteers":11,"sex":57,"minAge":269,"maxAge":270,"enrollmentInfo":271,"targetDuration":4,"studyType":22,"phases":273,"briefSummary":274,"conditions":275,"keywords":278,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":284,"lastUpdatePostDateStruct":285,"startDateStruct":286,"completionDateStruct":288,"leadSponsor":290,"locationsCount":48},"100615193","effect-of-a-mobile-app-for-obese-children-on-eating-attitudes-eating-awareness-and-healthy-eating-self-efficacy-100615193","NCT07289425","Effect of a Mobile App for Obese Children on Eating Attitudes, Eating Awareness, and Healthy Eating Self-Efficacy","The Effect of a Mobile Application Developed for Obese Children on Eating Attitudes, Eating Awareness, and Healthy Eating Self-Efficacy","Inclusion Criteria:\n\n* The child must be between 8 and 10 years old,\n* The child must not have any chronic illnesses other than obesity,\n* The child must be able to read and write in Turkish,\n* The child must be able to use a mobile device,\n* The child must not have a visual impairment,\n* The parent must be willing to participate in the study,\n* The parent must be able to read and write in Turkish,\n* The parent or child must have a smartphone.\n\nExclusion Criteria:\n\n* If they wish to withdraw from the study at any stage of the research,\n* If they do not wish to use the mobile application at any stage of the research.","8 Years","10 Years",{"count":272,"type":21},52,[24],"This study aims to evaluate the effect of a mobile application developed for obese children on eating attitudes, eating awareness, and healthy eating self-efficacy. The application seeks to support children in developing healthy eating habits and to integrate nursing interventions with digital health technologies in combating obesity. Data will be collected through a researcher-developed Information Form and three validated scales: the Eating Attitude Test, the Eating Awareness Scale, and the Healthy Eating Self-Efficacy Scale, completed by both children and parents.",[276,277],"Obesity","Child Health",[279,280,281,282,283],"Child health","obesity","eating behavior","mindful eating","self efficacy","2026-03-15",{"date":229,"type":40},{"date":287,"type":21},"2026-12-15",{"date":289,"type":21},"2027-06-15",{"name":46,"class":47},{"id":292,"slug":293,"hasResults":11,"nctId":294,"briefTitle":295,"officialTitle":296,"acronym":297,"eligibilityCriteria":298,"healthyVolunteers":11,"sex":57,"minAge":17,"maxAge":18,"enrollmentInfo":299,"targetDuration":4,"studyType":22,"phases":301,"briefSummary":302,"conditions":303,"keywords":308,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":314,"lastUpdatePostDateStruct":315,"startDateStruct":317,"completionDateStruct":319,"leadSponsor":320,"locationsCount":4},"100621743","impact-of-medication-education-on-adherence-and-side-effects-100621743","NCT07374588","Impact of Medication Education on Adherence and Side Effects","The Effect of Medication Education on Treatment Adherence and Side Effects in Psychiatric Inpatients: An Intervention Study","MED-ADHERE","Inclusion Criteria:\n\n* Adults aged 18-65 years\n* Hospitalized in a psychiatric inpatient clinic\n* Diagnosed with schizophrenia, schizoaffective disorder, schizophreniform disorder, bipolar disorder with psychotic features, or major depressive disorder with psychotic features\n* Receiving psychotropic medication treatment\n* Clinically stable and able to participate in educational sessions\n* Able to communicate verbally and understand the content of the education\n* Provided written informed consent\n\nExclusion Criteria:\n\n* Presence of severe cognitive impairment or intellectual disability\n* Acute medical or neurological conditions that may interfere with participation\n* Severe agitation or acute psychotic symptoms preventing participation\n* Hearing or communication impairments that limit participation in educational sessions\n* Participation in another psychosocial intervention study during the study period",{"count":300,"type":21},64,[24],"Severe mental disorders such as schizophrenia, bipolar disorder, and psychotic depression often require long-term or lifelong medication treatment. However, many psychiatric patients have difficulty adhering to their prescribed medication regimens due to factors such as lack of information, fear of side effects, and negative experiences with psychotropic medications. Poor treatment adherence is associated with symptom relapse, prolonged hospitalization, increased rehospitalization rates, reduced quality of life, and higher health care costs.\n\nMedication education is a key psychosocial intervention aimed at improving patients' understanding of their illness, treatment process, and potential medication side effects. Providing structured medication education may enhance treatment adherence and help patients recognize and manage side effects more effectively.\n\nThis intervention study aims to evaluate the effect of a structured medication education program on treatment adherence and medication-related side effects among psychotic inpatients hospitalized in a psychiatric clinic, including patients diagnosed with schizophrenia, schizoaffective disorder, schizophreniform disorder, bipolar disorder with psychotic features, and major depressive disorder with psychotic features. The findings of this study are expected to contribute to the development of effective psychosocial interventions to improve medication adherence and treatment outcomes in psychiatric inpatient settings.",[304,305,306,307],"Schizophrenia","Schizoaffective Disorder","Bipolar Disorder With Psychotic Features","Major Depressive Disorder With Psychotic Features",[309,310,311,312,313],"Medication Education","Psychiatric Inpatients","Psychoeducation","Treatment Adherence","Medication Side Effects","2026-01-24",{"date":316,"type":40},"2026-01-29",{"date":318,"type":21},"2026-01-02",{"date":120,"type":21},{"name":46,"class":47},{"id":322,"slug":323,"hasResults":11,"nctId":324,"briefTitle":325,"officialTitle":326,"acronym":4,"eligibilityCriteria":327,"healthyVolunteers":11,"sex":57,"minAge":17,"maxAge":4,"enrollmentInfo":328,"targetDuration":4,"studyType":22,"phases":329,"briefSummary":330,"conditions":331,"keywords":334,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":339,"lastUpdatePostDateStruct":340,"startDateStruct":342,"completionDateStruct":343,"leadSponsor":345,"locationsCount":48},"100610915","comparison-of-acb-with-acb-and-bifes-combination-in-knee-arthroplasty-surgeries-100610915","NCT07233785","Comparison of ACB With ACB and BiFeS Combination in Knee Arthroplasty Surgeries","Comparison of the Postoperative Analgesic Efficacy of the Combination of Adductor Canal Block and Biceps Femoris Short Head Block Versus Adductor Canal Block Alone in Patients Undergoing Total Knee Arthroplasty","Inclusion Criteria:\n\n* Adult patients over 18 years of age who underwent percutaneous nephrolithotomy under general anesthesia and were I-II-III according to the American Society of Anesthesiologists (ASA) risk classification were included in the study.\n\nExclusion Criteria:\n\n* patients who did not give consent,\n* patients with coagulopathy,\n* patients with signs of infection at the block application site,\n* patients using anticoagulants,\n* patients with known allergies to any of the study drugs,\n* patients with unstable hemodynamics,\n* patients who could not cooperate during postoperative pain assessment\n* patients who wanted to withdraw from the study,\n* patients with alcohol and drug addiction,\n* patients with musculoskeletal abnormalitie",{"count":137,"type":21},[24],"The aim is to compare the postoperative analgesic effects of Adductor Canal and Biceps Femoris Short Head Blocks with Adductor Canal Block in patients undergoing Knee Arthroplasty surgery",[114,332,333],"Knee Surgery","Knee Arthroplasty, Total",[31,335,336,337,338,32],"knee arthroplasty","biceps femoris short head","bifes","adductor canal blok","2025-11-20",{"date":341,"type":40},"2025-11-25",{"date":339,"type":21},{"date":344,"type":21},"2026-11-25",{"name":46,"class":47},{"id":347,"slug":348,"hasResults":11,"nctId":349,"briefTitle":350,"officialTitle":351,"acronym":4,"eligibilityCriteria":352,"healthyVolunteers":11,"sex":57,"minAge":17,"maxAge":353,"enrollmentInfo":354,"targetDuration":4,"studyType":22,"phases":355,"briefSummary":356,"conditions":357,"keywords":359,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":362,"lastUpdatePostDateStruct":363,"startDateStruct":365,"completionDateStruct":367,"leadSponsor":369,"locationsCount":48},"100610912","comparison-of-qipb-and-sificb-in-hip-surgery-100610912","NCT07233746","Comparison of QIPB and SIFICB in Hip Surgery","Comparison of the Effects of Quadroiliac Plane Block Versus Suprainguinal Fascia Iliaca Compartment Block on Postoperative Pain in Hip Surgery","Inclusion Criteria:\n\n* Adult patients over 18 years of age who underwent percutaneous nephrolithotomy under general anesthesia and were I-II-III according to the American Society of Anesthesiologists (ASA) risk classification were included in the study.\n\nExclusion Criteria:\n\n* patients who did not give consent,\n\n  * patients with coagulopathy,\n  * patients with signs of infection at the block application site,\n  * patients using anticoagulants,\n  * patients with known allergies to any of the study drugs,\n  * patients with unstable hemodynamics,\n  * patients who could not cooperate during postoperative pain assessment\n  * patients who wanted to withdraw from the study,\n  * patients with alcohol and drug addiction,\n  * patients with musculoskeletal abnormalitie","99 Years",{"count":137,"type":21},[24],"The aim is to compare the postoperative analgesic effects of Quadroiliac Plane Block (QIPB) and Suprainguinal Fascia Iliaca Compartment Block (SIFICB) in patients undergoing hip surgery.",[141,358],"Hip Surgery",[31,360,32,145,361],"hip surgery","suprainguinal fascia iliaca compartment block","2025-11-14",{"date":364,"type":40},"2025-11-18",{"date":366,"type":21},"2025-12-15",{"date":368,"type":21},"2026-05",{"name":46,"class":47},{"id":371,"slug":372,"hasResults":11,"nctId":373,"briefTitle":374,"officialTitle":374,"acronym":375,"eligibilityCriteria":376,"healthyVolunteers":11,"sex":57,"minAge":17,"maxAge":18,"enrollmentInfo":377,"targetDuration":4,"studyType":22,"phases":379,"briefSummary":380,"conditions":381,"keywords":385,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":389,"lastUpdatePostDateStruct":390,"startDateStruct":392,"completionDateStruct":394,"leadSponsor":396,"locationsCount":48},"100588630","investigation-of-the-acute-effects-of-core-stabilization-and-360-degree-breathing-exercises-on-balance-and-proprioception-in-individuals-with-non-specific-low-back-pain-100588630","NCT06943898","Investigation of the Acute Effects of Core Stabilization and 360-Degree Breathing Exercises on Balance and Proprioception in Individuals With Non-Specific Low Back Pain","360° Breath","Inclusion Criteria:\n\n* Low back pain persisting for at least 3 months\n* No neurological, rheumatological, or musculoskeletal system problems\n\nExclusion Criteria:\n\n* Individuals with neurological, vestibular, or serious orthopedic conditions that may cause physical disability\n* Patients with back-leg or dorsolumbar pain due to lumbar disc protrusion or fracture\n* Cancer patients\n* Individuals with acute infections\n* Individuals with respiratory system diseases\n* Individuals with any mental disorder that would prevent participation in the study assessment\n* Pregnant individuals",{"count":378,"type":21},46,[24],"This study is designed as a single-blind randomized controlled trial. Male and female patients aged 18-65 years with complaints of non-specific low back pain (NSLBP) lasting longer than 12 weeks will be included in the study. Participants will be randomly assigned into two parallel groups: control and intervention. The control group will perform core stabilization exercises five days a week for three weeks. In the intervention group, core stabilization exercises will be combined with 360-degree breathing exercises. To our knowledge, there is no randomized controlled trial investigating the effect of combining core stabilization with 360-degree breathing in individuals with NSLBP. The aim of this study is to examine the acute effects of combining 360-degree breathing techniques with core stabilization exercises on balance and proprioception in individuals with NSLBP.",[382,383,384],"Low Back Pain (LBP)","Exercise","Core Stability",[386,387,388],"core stability exercise","low back pain","exercise","2025-08-01",{"date":391,"type":40},"2025-08-06",{"date":393,"type":40},"2025-07-30",{"date":395,"type":21},"2025-12-01",{"name":46,"class":47},{"id":398,"slug":399,"hasResults":11,"nctId":400,"briefTitle":401,"officialTitle":402,"acronym":403,"eligibilityCriteria":404,"healthyVolunteers":56,"sex":57,"minAge":17,"maxAge":405,"enrollmentInfo":406,"targetDuration":4,"studyType":22,"phases":407,"briefSummary":408,"conditions":409,"keywords":412,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":418,"lastUpdatePostDateStruct":419,"startDateStruct":421,"completionDateStruct":423,"leadSponsor":425,"locationsCount":48},"100593266","arcs-based-training-to-improve-nursing-students-communication-motivation-and-self-efficacy-100593266","NCT07004205","ARCS-Based Training to Improve Nursing Students' Communication, Motivation, and Self-Efficacy","The Effect of Training Based on the ARCS Motivation Model on Nursing Students' Communication Skills, Learning Motivation, and Self-Efficacy: A Randomized Controlled Trial","ARCS-NCOMSE","Inclusion Criteria\n\n* Must be enrolled in the 1st year of the Nursing Faculty\n* Must be participating in clinical practice (internship) for the first time\n* Must voluntarily agree to participate in the study and sign the informed consent form\n* Must agree to attend all designated sessions during the training period\n* Must have proficiency in reading and writing Turkish\n* Must have a suitable health condition for participation in individual and group activities\n\nExclusion Criteria:\n\nHas previously participated in any clinical practice\u002Finternship\n\n* Has previously attended specialized training on communication skills, self-efficacy, or learning motivation\n* Unable to attend 2 or more sessions during the research process\n* Decides to withdraw from participation during the research or withdraws consent\n* Provides incomplete or incorrect responses to data (significant omissions in pre-test or post-test forms)","20 Years",{"count":137,"type":21},[24],"This study explores the impact of an ARCS-based training program on nursing students' communication skills, learning motivation, and self-efficacy. Communication is essential in nursing for quality patient care and safety, yet students often struggle with it. The ARCS Motivation Model-focused on Attention, Relevance, Confidence, and Satisfaction-aims to boost motivation and improve learning outcomes. Using a randomized controlled design, the study compares an experimental group receiving ARCS-based training with a control group receiving traditional education. Key outcomes include improved communication skills, motivation, and self-efficacy. This research highlights the potential of the ARCS model in enhancing nursing education and student performance.",[410,411],"Educational Intervention","Motivation Model",[413,414,415,416,417],"ARCS Motivation Model","nursing students","communication skills","learning motivation","self-efficacy levels","2025-06-16",{"date":420,"type":40},"2025-06-19",{"date":422,"type":40},"2025-05-26",{"date":424,"type":21},"2025-06-20",{"name":46,"class":47},{"id":427,"slug":428,"hasResults":11,"nctId":429,"briefTitle":430,"officialTitle":431,"acronym":432,"eligibilityCriteria":433,"healthyVolunteers":56,"sex":57,"minAge":17,"maxAge":434,"enrollmentInfo":435,"targetDuration":4,"studyType":22,"phases":437,"briefSummary":438,"conditions":439,"keywords":442,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":448,"lastUpdatePostDateStruct":449,"startDateStruct":451,"completionDateStruct":453,"leadSponsor":455,"locationsCount":128},"100593263","effects-of-tpr-and-z-techniques-on-pain-and-drug-leakage-in-intramuscular-injections-100593263","NCT07004166","Effects of TPR and Z Techniques on Pain and Drug Leakage in Intramuscular Injections","Effects of TPR Technique and Z Technique on Pain and Drug Leakage in Intramuscular Injections","TPR_Z_PainLeak","Inclusion Criteria:\n\n* Aged 16-40\n* Prescribed diclofenac sodium\n* No communication impairments\n* Healthy ventrogluteal muscles without sensory issues\n\nExclusion Criteria:\n\n* Wounds, redness, bruising, tenderness, or stiffness at the injection site\n* Injection in the past 2 weeks\n* Neuropathy or other medical conditions\n* BMI below 15 or above 35","40 Years",{"count":436,"type":21},76,[24],"This randomized, triple-blind clinical trial compares the effectiveness of Z-track and TPR (traction-pressure-release) techniques in reducing pain and medication leakage during ventrogluteal intramuscular injections. Pain is measured using VAS, and leakage is assessed with a millimeter scale. The study aims to identify a more efficient, less painful injection method.",[440,441],"Muscle Pain","Injection Site Pain",[443,444,445,446,447],"Intramuscular Injection","Drug Leakage l","Pain","Z-Track","TPR Techniques","2025-06-03",{"date":450,"type":40},"2025-06-04",{"date":452,"type":21},"2025-06-15",{"date":454,"type":21},"2025-08-25",{"name":46,"class":47},{"id":457,"slug":458,"hasResults":11,"nctId":459,"briefTitle":460,"officialTitle":461,"acronym":4,"eligibilityCriteria":462,"healthyVolunteers":56,"sex":57,"minAge":17,"maxAge":463,"enrollmentInfo":464,"targetDuration":4,"studyType":22,"phases":465,"briefSummary":466,"conditions":467,"keywords":469,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":473,"lastUpdatePostDateStruct":474,"startDateStruct":476,"completionDateStruct":478,"leadSponsor":480,"locationsCount":48},"100579871","the-effect-of-e-booklet-tranng-on-self-effcacy-and-comfort-level-in-patents-wth-urnary-catheter-100579871","NCT06829927","The Effect of E-Booklet Traınıng on Self-Effıcacy and Comfort Level in Patıents Wıth Urınary Catheter","The Effect of E-Booklet Traınıng Created Wıthın the Scope of Comfort Theory on Self-Effıcacy and Comfort Levels in Patıents Wıth Urınary Catheter: a Randomızed Controlled Study","Inclusion Criteria:\n\nPatients who can actively use information technologies such as phones and tablets\n\n* Inpatients in the Urology Clinic\n* Conscious and oriented patients\n* Patients aged 18-75 years\n* Patients with short-term catheterization\n* Patients without hearing and communication disabilities\n* Literate patients\n\nExclusion Criteria:\n\n* Patients who incompletely completed the data collection tool\n* Patients with hearing, vision and comprehension problems,","75 Years",{"count":217,"type":21},[24],"Urinary catheterization is the insertion of a tube through the urethra into the bladder to empty or flush the bladder. Catheterization is preferred in patients with urinary retention and urinary incontinence, in patients who will undergo surgical intervention or in cases where a procedure needs to be performed in the urinary tract, and is applied for short (1-7 days), medium (7-28 days) and long term (longer than 28 days) (National Institute of Diabetes and Digestive and Kidney Diseases. (2023). Urinary catheterization is frequently preferred in applications related to treatment and care. According to the CAUTI report, the frequency of urinary catheterization in hospitalized patients in one year is between 15-25% in the world. This rate is between 10-15% in developed countries and 20-30% in developing countries (CAUTI, 2015).",[468],"Urinary Catheter",[470,471,472],"urinary cathether","comfort","self-efficiaty","2025-02-11",{"date":475,"type":40},"2025-02-17",{"date":477,"type":40},"2024-09-15",{"date":479,"type":21},"2025-12-30",{"name":46,"class":47},{"id":482,"slug":483,"hasResults":11,"nctId":484,"briefTitle":485,"officialTitle":486,"acronym":4,"eligibilityCriteria":487,"healthyVolunteers":56,"sex":57,"minAge":17,"maxAge":488,"enrollmentInfo":489,"targetDuration":4,"studyType":22,"phases":491,"briefSummary":492,"conditions":493,"keywords":495,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":499,"lastUpdatePostDateStruct":500,"startDateStruct":502,"completionDateStruct":504,"leadSponsor":506,"locationsCount":48},"100567010","analgesic-effect-of-m-tapa-and-tapb-on-laparoscopic-cholesistectomy-100567010","NCT06662617","Analgesic Effect of M-TAPA and TAPB on Laparoscopic Cholesistectomy","Comparison of the Effects of M-TAPA and TAP Nerve Block Applications on Postoperative Pain Scores and Analgesia Requirements in Laparoscopic Cholecystectomy","Inclusion Criteria:\n\n* Adult patients older than 18 years of age who underwent elective laparoscopic cholecystectomy under general anesthesia and were American Society of\n* Anesthesiologists (ASA) I-II-III according to the ASA risk classification.\n\nExclusion Criteria:\n\n* Patients who did not give consent,\n* patients with coagulopathy,\n* patients with signs of infection at the block application site,\n* patients using anticoagulants,\n* patients with local anesthetic drug allergies,\n* patients undergoing open surgery,\n* patients with unstable hemodynamics,\n* patients who could not cooperate during postoperative pain assessment","80 Years",{"count":490,"type":21},12,[24],"Cholecystectomy is the most frequently performed abdominal surgery in developed nations, with laparoscopic cholecystectomy being recognized as the gold standard technique for treating gallstones.\n\nThe efficacy of TAP block for pain relief has been well-documented following laparoscopic cholecystectomy procedures. Recently, m-TAPA block has emerged as an alternative analgesic technique for abdominal surgeries.\n\nThis study aims to evaluate and compare the effectiveness of these two analgesic methods in managing postoperative pain after laparoscopic cholecystectomy.",[494],"Post Operative Pain",[496,497,498],"laparoscopic cholecystectomy","m-tapa","tap","2024-11-04",{"date":501,"type":40},"2024-11-06",{"date":503,"type":40},"2024-11-01",{"date":505,"type":21},"2025-01-01",{"name":46,"class":47},{"id":508,"slug":509,"hasResults":11,"nctId":510,"briefTitle":511,"officialTitle":512,"acronym":4,"eligibilityCriteria":513,"healthyVolunteers":11,"sex":57,"minAge":17,"maxAge":514,"enrollmentInfo":515,"targetDuration":4,"studyType":22,"phases":517,"briefSummary":518,"conditions":519,"keywords":520,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":526,"lastUpdatePostDateStruct":527,"startDateStruct":529,"completionDateStruct":531,"leadSponsor":533,"locationsCount":4},"100558627","comparison-of-psb-and-rifpb-combination-with-psb-and-espb-combination-in-cardiac-surgery-with-sternotomy-100558627","NCT06553573","Comparison of PSB and RIFPB Combination With PSB and ESPB Combination in Cardiac Surgery With Sternotomy","Postoperative Analgesic Efficacy Comparison of a Combination of Superficial Parasternal Block (PSB) and Recto-intercostal Fascial Plane Block (RİFPB) Versus a Combination of Erector Spinae Plane Block (ESPB) and Superficial Parasternal Block (PSB) in Patients Undergoing Cardiac Surgery With Sternotomy.","Inclusion Criteria:\n\n* Adult patients over 18 years of age who will undergo cardiac surgery with sternotomy under general anesthesia and who are in classes I-IIIII according to the American Society of Anesthesiologists (ASA) risk classification.\n\nExclusion Criteria:\n\n* Patients who did not give consent,\n* patients with coagulopathy,\n* patients with signs of infection at the block application site,\n* patients using anticoagulants,\n* patients with local anesthetic drug allergies,\n* patients with unstable hemodynamics,\n* patients who could not cooperate during postoperative pain assessment","85 Years",{"count":516,"type":21},24,[24],"The goal of this study is to compare the analgesic efficacy of the combination of PSB and RIFPB and the combination of PSB and ESPB in patients undergoing cardiac surgery with sternotomy.",[494],[521,522,523,524,525,32,31],"sternotomy","cardiac surgery","parasternal block","recto-intercostal fascial plane block","erector spinae plane block","2024-08-12",{"date":528,"type":40},"2024-08-14",{"date":530,"type":21},"2024-08-15",{"date":532,"type":21},"2024-09-20",{"name":46,"class":47},{"id":535,"slug":536,"hasResults":11,"nctId":537,"briefTitle":538,"officialTitle":539,"acronym":4,"eligibilityCriteria":540,"healthyVolunteers":11,"sex":57,"minAge":17,"maxAge":514,"enrollmentInfo":541,"targetDuration":4,"studyType":22,"phases":543,"briefSummary":544,"conditions":545,"keywords":546,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":526,"lastUpdatePostDateStruct":547,"startDateStruct":548,"completionDateStruct":549,"leadSponsor":550,"locationsCount":4},"100558626","the-efficacy-of-psb-and-recto-intercostal-block-combination-on-postoperative-pain-in-patients-undergoing-cardiac-surgery-via-sternotomy-case-series-100558626","NCT06553560","The Efficacy of PSB and Recto-intercostal Block Combination on Postoperative Pain in Patients Undergoing Cardiac Surgery Via Sternotomy: Case Series","Investigation of the Postoperative Analgesic Effect of the Combination of Superficial Parasternal Block (PSB) and Recto-Intercostal(İC) Fascial Plane Block in Patients Undergoing Cardiac Surgery Via Sternotomy: Case Series","Inclusion Criteria:\n\n* Adult patients over 18 years of age who will undergo cardiac surgery with sternotomy under general anesthesia and who are in classes I-II-III according to the American Society of Anesthesiologists (ASA) risk classification.\n\nExclusion Criteria:\n\n* Patients who did not give consent,\n\n  * patients with coagulopathy,\n  * patients with signs of infection at the block application site,\n  * patients using anticoagulants,\n  * patients with local anesthetic drug allergies,\n  * patients with unstable hemodynamics,\n  * patients who could not cooperate during postoperative pain assessment",{"count":542,"type":21},10,[24],"The aim of this study was to investigate the effectiveness of the combination of Superficial Parasternal Block and Recto-Intercostal Fascial Plane Block in patient groups undergoing cardiac surgery via sternotomy by evaluating postoperative pain scores and analgesic consumption.",[494],[521,522,523,524,31,32],{"date":528,"type":40},{"date":530,"type":21},{"date":532,"type":21},{"name":46,"class":47},{"id":552,"slug":553,"hasResults":11,"nctId":554,"briefTitle":555,"officialTitle":556,"acronym":4,"eligibilityCriteria":557,"healthyVolunteers":11,"sex":57,"minAge":17,"maxAge":514,"enrollmentInfo":558,"targetDuration":4,"studyType":22,"phases":560,"briefSummary":561,"conditions":562,"keywords":563,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":566,"lastUpdatePostDateStruct":567,"startDateStruct":569,"completionDateStruct":571,"leadSponsor":573,"locationsCount":4},"100553245","comparison-of-m-tapa-and-tap-blocks-on-postoperative-analgesia-in-laparoscopic-appendectomy-surgeries-100553245","NCT06483581","Comparison of M-TAPA and TAP Blocks on Postoperative Analgesia in Laparoscopic Appendectomy Surgeries","Comparison of the Analgesic Effects of Modified Thoracoabdominal Nerve Block Through Pericondrial Approach (M-TAPA) and Transversus Abdominis Plane (TAP) Block in Laparoscopic Appendectomy Surgeries","Inclusion Criteria:\n\n* Adult patients older than 18 years of age who will undergo laparoscopic appendectomy under general anesthesia and will be American Society of Anesthesiologists (ASA) I-II-III according to the ASA risk classification.\n\nExclusion Criteria:\n\n* Patients who did not give consent,\n* patients with coagulopathy,\n* patients with signs of infection at the block application site,\n* patients using anticoagulants,\n* patients with local anesthetic drug allergies,\n* patients undergoing open surgery,\n* patients with unstable hemodynamics,\n* patients who could not cooperate during postoperative pain assessment",{"count":559,"type":21},30,[24],"The goal of this study is to compare the analgesic efficacy of M-TAPA block and TAP block in patients undergoing laparoscopic appendectomy surgeries",[494],[497,564,565,32,31],"tap block","laparoscopic appendectomy","2024-07-01",{"date":568,"type":40},"2024-07-03",{"date":570,"type":21},"2024-07",{"date":572,"type":21},"2024-09",{"name":46,"class":47},""]